US20130217769A1 - Pharmaceutical semi-solid composition of isotretinoin - Google Patents

Pharmaceutical semi-solid composition of isotretinoin Download PDF

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US20130217769A1
US20130217769A1 US13/713,897 US201213713897A US2013217769A1 US 20130217769 A1 US20130217769 A1 US 20130217769A1 US 201213713897 A US201213713897 A US 201213713897A US 2013217769 A1 US2013217769 A1 US 2013217769A1
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pharmaceutical composition
oral pharmaceutical
composition
isotretinoin
low dose
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US9089534B2 (en
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Francis Vanderbist
Cécile Servais
Phillippe Baudier
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GALEPHAR PHARMACEUTICAL RESEARCH Inc
Galephar P R Inc Ltd
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Galephar MF
Galephar P R Inc Ltd
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/203—Retinoic acids ; Salts thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/202—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/44—Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/4858—Organic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/4866—Organic macromolecular compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/10—Anti-acne agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
    • A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers

Definitions

  • the present invention relates to an oral pharmaceutical composition of isotretinoin containing at least two excipients, one of them being hydrophilic (i.e. having an HLB value superior or equal to 10), the other being an oily vehicle.
  • Isotretinoin 13-cis retinoic acid or 13-cis vitamin A
  • isomers and some of its analogs are widely known to have a therapeutical activity in the treatment of several severe skin disorders like cystic acne, hypertrophic lupus erythematosus, keratinization disorders.
  • Some evidences have also been brought about the activity of isotretinoin in basal cell carcinoma and squamous cell carcinoma.
  • isotretinoin is also a highly toxic drug. Indeed, although isotretinoin, which is a cis derivative, is known to be less toxic than all trans vitamin A derivatives, side effects resulting from its use such as headache, vomiting, irritation of mucosa and liver toxicity, occur frequently. Furthermore, isotretinoin is known to be highly teratogenic in both animals and humans.
  • Isotretinoin is a reddish-orange powder. It is decomposed in presence of light and atmospheric oxygen. Isotretinoin is very poorly soluble in water what made its bioavailability quite low after an oral intake (25% in fasted conditions and 40% in fed conditions).
  • the maximum concentration (C max ) is reached after 2-4 hours, while the (C max ) of the active metabolite, 4-oxo-isotretinoin is reached after 6 hours.
  • the elimination half-life of isotretinoin is of 7 to 37 hours while the half life (t 1/2 ) of the active metabolite is of 11 to 50 hours.
  • the steady-state concentrations of isotretinoin are reached after 1 week of treatment.
  • the EP patent 0184942 describes more specific compositions of isotretinoin involving the use of one antioxidant, one chelating agent, one pharmaceutical carrier and one suspending agent. The composition obtained is stable during time.
  • the U.S. Pat. No. 4,545,977 relates to improved compositions of isotretinoin wherein taurine is associated with isotretinoin to reduce the side effects thereof.
  • the U.S. Pat. No. 5,716,928 describes a method for increasing bioavailability and for reducing inter and intra individual variability of an orally administered hydrophobic pharmaceutical compound, which comprises orally administering the pharmaceutical compound with an essential oil or essential oil component in an amount sufficient to provide greater bioavailability of the active ingredient.
  • the U.S. Pat. No. 6,028,054 relates to a method for increasing bioavailability of an orally administered hydrophobic pharmaceutical compound to human, which comprises orally administering the pharmaceutical compound concurrently with a bioenhancer comprising an inhibitor of e-cytochrome P450 3A enzyme or an inhibitor of P-glycoprotein mediated membrane transport.
  • the U.S. Pat. No. 5,993,858 describes a self microemulsifying excipient formulation for increasing the bioavailability of a drug which includes an emulsion including an oil or other lipid material, a surfactant and an hydrophilic co-surfactant.
  • compositions of isotretinoin containing at least two lipid materials, one of them being hydrophilic.
  • the said composition may be a suspension, emulsion or microemulsion.
  • Isotretinoin is characterized by a low absolute bioavailability and a high inter and intra individual variability. Isotretinoin also presents a wide range of side effects among which some are severe (ocular, skin anemia, hepatic, . . . ). It is consequently of a particular interest to dispose of a reliable, stable and highly bioavailable formulation of isotretinoin.
  • a semi-solid dosage form containing isotretinoin is a form in which isotretoin is mixed with suitable melted excipients. The molten mix is then filled for example into hard gelatine capsules or other pharmaceutically acceptable capsules. At ambient temperature (temperature for example of less than 20° C.), the content of the capsule is solid while at temperature higher than 20° C. (for example at temperature greater or equal to 30° C., advantageously greater or equal to 35° C., preferably substantially at body temperature+/ ⁇ 37° C.), it is liquid or semi-solid (paste).
  • the isotretinoin may be solubilized in the mix of excipients or partially solubilized.
  • the active ingredient may also be formulated as a suspension, emulsion or microemulsion.
  • Various lipidic excipients are available to the formulator to obtain a semi-solid formulation.
  • Excipients compatible with hard gelatin capsule shells are: lipophilic liquid vehicles (refined specialty oils, medium-chain triglycerides and related esters), semi-solid lipophilic vehicles, solubilizing agents, emulsifying agents and absorption enhancers.
  • the classification of fatty excipients is based on the hydrophilicity or lipophilicity of the excipients, characterized by the hydrophilic/lipophilic balance value (HLB).
  • lipophilic excipients are vegetable oils (peanut oil, olive oil, soyabean oil, . . . ), fatty acids (stearic acid, palmitic acid, . . . ), fatty alcohols, . . .
  • hydrophilic excipients are polyethyleneglycol (PEG) with a molecular weight superior to 3,000.
  • the advantages of the semi-solid formulations of the invention are multiple for isotretinoin: protection of the active ingredient from air and humidity, possibility of increasing the dissolution rate of the molecule and hence of the bioavailability, diminution of the risk of contamination of the operator, diminution of the risk of cross contamination, no possibility of demixing under the effect of vibrational mixing during manufacturing process, facility of the production process.
  • the choice of the nature of the formulation of course influenced the stability of the pharmaceutical form and the bioavailability of the isotretoin contained in it.
  • a maximum bioavailability is achieved by preparing and keeping the drug in the amorphous/solubilized state in a solid dispersion or in a lipid-based formulation.
  • the barrier we are avoiding is the compound a washing-out a of solution to a large extent into a insoluble crystalline form during the dissolution/release step in vivo.
  • These systems may consist of suspension, emulsion, microemulsion, self-emulsifying drug delivery systems (SEDDS®) or self-emulsifying microemulsion drug delivery system (SMEDDS®).
  • SEDDS® self-emulsifying drug delivery systems
  • SMEDDS® self-emulsifying microemulsion drug delivery system
  • Microemulsions have the added advantage over suspensions such as emulsions and dispersions since thermodynamically they are more stable, that they can be manufactured with little energy input and have generally a longer shelf-life. Nevertheless, a microemulsion formulation is not a guarantee of higher bioavailability in comparison to suspension a described hereafter.
  • oil-in-water (O/W) and water-in-oil (W/O) microemulsions usually involves a combination of 3-5 basic compounds i.e. oil, surfactant, cosurfactant, water and electrolytes.
  • the challenge is to select for a particular application oil(s) and surfactant(s) that are acceptable from a toxicological perspective and that allow to obtain a high bioavailability of the drug, i.e isotretoin.
  • the pharmaceutical composition of the invention is an oral semi-solid pharmaceutical composition of isotretinoin containing two lipidic excipients, one of them being hydrophilic i.e. having a HLB value of at least 10, for example equal to 10, but preferably greater than 10, such as greater or equal to 12, for example comprised between 12 and 14, and the other being an oily vehicle.
  • the pharmaceutical composition of the invention contains advantageously at least one hydrophilic excipient with a HLB value of at least 10 selected from the group consisting of glyceroyl macrogoiglycerides, polyethyleneglycol derivatives, and mixtures thereof.
  • the pharmaceutical composition contains from 20 to 80% by weight of hydrophilic excipient with a HLB value of at least 10 selected from the group consisting of glyceroyl macrogolglycerides, polyethyleneglycol derivatives, and mixtures thereof.
  • the oily vehicle is selected from the group consisting of vegetable oils, medium chain triglycerides, fatty acid esters, amphiphilic oil, glycerol oleate derivative, and mixtures thereof.
  • the composition contains from 5 to 70% by weight of an oily vehicle selected from the group consisting of vegetable oils, medium chain triglycerides, fatty acid esters, amphiphilic oil, glycerol oleate derivative, and mixtures thereof.
  • the composition further contains at least one surfactant, preferably selected from the group consisting of sorbitan fatty acid esters, polysorbate derivatives, polyoxyethylene sorbitan fatty acid esters, sodium laurylsulphate, derivatives of lecithine, propylene glycol esters, fatty acid esters of propylene glycol, fatty acid esters of glycerol, polyethylene glycol, and mixtures thereof.
  • the composition contains from 1 to 10% by weight of at least one surfactant.
  • the pharmaceutical formulation of the invention contains advantageously at least one disintegrant, preferably selected from the group consisting of povidone derivative, sodium croscarmellose and mixtures thereof.
  • the pharmaceutical composition of the invention may contain one or more surfactants and/or one or more disintegrants, but contains preferably one or more compounds acting as surfactants and one or more compounds acting as disintegrants.
  • the invention relates also to a pharmaceutical acceptable capsule containing at least one semi-solid composition of the invention, for example at least one composition of the invention as disclosed hereabove.
  • the capsule is for example selected from the group consisting of hard gelatine capsules, soft gelatine capsules, hypromellose capsules, starch capsules.
  • FIG. 1 is a ternary diagram of a formulation containing only Gelucire® 50/13 and soyabean oil, the third component being water;
  • FIG. 2 shows the dissolution rate of a reference product (Roaccutane®-20 mg active agent), of a suspension containing 20 mg Isotretoin and of an emulsion SEDDS® containing 10 mg Isotretoin;
  • FIG. 3 shows an in vivo comparative pharmacokinetic profile of isotretinoin
  • FIG. 4 gives the comparative pharmacokinetic profile of different formulations for isotretinoin
  • FIG. 5 gives the comparative pharmacokinetic profile of different formulations for 4-oxo-isotretinoin, the active metabolite of isotretinoin and
  • FIGS. 6 and 7 describe the mean pharmacokinetic profile of isotretinoin and 4-oxoisotretinoin for two formulations.
  • the present invention relates thus to a semi-solid formulation of isotretinoin containing at least 2 lipidic excipients, one of them being an hydrophilic excipient (having a high HLB value namely >10) and the other an oily excipient.
  • the molten mix of these two excipients allows to totally or partially (depending on the ratio between excipients) dissolve isotretinoin.
  • Different kinds of formulations (SEDDS® or suspensions) of isotretinoin have been formulated. For suspensions, it was possible to dissolve a high fraction of isotretinoin in the mix of excipients and even the whole quantity of the active ingredient if the manufacturing conditions (high temperature and long time of mixing) and the formulations were optimized.
  • Excipients particularly suitable for the dissolution of isotretinoin were lauroyl Macrogol-32 glycerides (Gelucire® 44/14, Gattefossé) and Stearoyl Macrogol-32 glycerides (Gelucire® 50/13, Gattefossé).
  • hydrophilic components When those hydrophilic components are melted together with an oily vehicle, it allows to obtain very stable suspensions of isotretinoin in which an important part of the active ingredient is dissolved.
  • a surfactant may also be added to the formulation to still improve the physical stability of the suspension.
  • SEDDS® formulations of isotretinoin are also stable and may give an improved bioavailability of the drug.
  • Ternary diagrams allow to observe different areas corresponding to different physical states namely coarse emulsion, true emulsion, lamellar solution or micellar solution when the ratio between excipients changes.
  • FIG. 1 The behaviour of the formulation in presence of water changes when the ratio changes.
  • FIG. 1 One example of this ternary diagram is given in FIG. 1 for a formulation of isotretinoin containing Gelucire® 50/13 and soyabean oil.
  • the effect of different lipophilic excipients was evaluated in the form of semi-solid capsules.
  • the semi-solid capsules were made by addition of the active substance at the pre-melted lipophilic compounds followed by the filling of the liquid into hard gelatin capsule.
  • the active substance was incorporated into formulations, listed in table I, consisting of glyceroyl macrogolglyceride associated with soyabean oil or derivative, medium chain triglyceride.
  • stearoyl macroglyceride (Gélucire® 50/13, Gattefosse) and soyabean oil allows to obtain a formulation with a dissolution profile similar to the reference (Roaccutane® 20 mg, Roche).
  • an oily excipient can improve the absorption of lipophilic drug by increasing the solubility of the drug in the lipidic phase, but the release of the active ingredient from the formulation can be slowed down due to the high affinity of the drug for the oily phase.
  • dispersed systems emulsions or suspensions
  • lipophilic or hydrophilic vehicles improves the absorption of the drug as well as increasing a larger contact surface.
  • the drug release profiles of the formulations 1 to 5 were evaluated in phosphate buffer pH 7.5 with laurylsulfate and pancreatin. The percent of isotretinoin released after 4 hours is given in the following table II.
  • Stearoyl macrogolglyceride (Gelucire® 50/13) known as a drug solubilizer and emulsifying agent of different drugs (in SMEDDS® or SEDDS®) was tested in association with soyabean oil.
  • This component has the ability to solubilize a great part of isotretinoin in the formulation.
  • the percentage of isotretinoin released increases generally with the percentage of Gelucire® in the formulation (increased solubility of the active in this vehicle).
  • the formulation 3 ratio oil/Gelucire® 50/13:0.2
  • the prediction power of the in vitro dissolution test is weak since the in vitro/in vivo correlation is known to be poor. Nevertheless, an optimized dissolution test (using enzymes and surfactant) is of some help to assess the rate of release of the drug from the lipidic composition. It must be noted that the conditions of the dissolution (dissolution medium, speed of the paddles, temperature . . . ) test influence dramatically the results of the test and should consequently be standardized to allow comparison between various formulations.
  • FIG. 2 shows the dissolution rate of a reference product (Roaccutane®-20 mg active agent), of a suspension containing 20 mg Isotretoin and of an emulsion SEDDS®containing 10 mg Isotretoin (formulation given hereinbelow).
  • the caco-2 cell culture system can be used for determining permeability of compounds (especially for poorly soluble compounds).
  • the caco-2 cell model allows to measure the transport of drug from the apical to the serosal side as well as from the serosal to the apical side. This allows to determine if an efflux system is operational.
  • the caco-2 cells model is interesting because:
  • the formulations tested are put in solution in 250 ml of BME. Taurocholate (10 mM) was added to the solutions to better mimate the in physiological conditions. The different solutions so prepared are put in contact with Caco-2 cells at the apical or basolateral side. The cells culture inserts) are incubated for 3 hours at 37° C. and samples of 100 ⁇ l are taken every hours
  • Soyabean oil 270 mg
  • FIG. 3 described the mean pharmacokinetic profile obtained for each formulation.
  • suspension and SEDDS® formulations both presented a lower intraindividual variability of the bioavailability as demonstrated by the values of relative standard deviations (rsd) which are of 36.0%, 22.72% and 28.18% for Roaccutane® 20 mg, suspension 20 mg and SEDDS® 10 mg respectively.
  • Soyabean oil 133 mg
  • Soyabean oil 130 mg
  • FIG. 4 gives the comparative pharmacokinetic profile of each formulation for isotretinoin
  • FIG. 5 gives the comparative pharmacokinetic profile of each formulation for 4-oxo-isotretinoin, the active metabolite of isotretinoin.
  • bioavailability of a capsule of isotretinoin 16 mg has been assessed and compared to the bioavailability of the reference (ROACCUTANE® 20 mg capsule, Roche) on 24 healthy subjects.
  • the subjects were healthy caucasian volunteers of both sexes (non-pregnant, non-breast-feeding), aged 18 to 50 years, non smokers or smoking less than 10 cigarettes per day.
  • the drugs was taken with food (a standardized breakfast).
  • Blood samples were collected according to the following sampling schedule: pre-dose and 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 10 h, 12 h, 14 h, 24 h, 36 h, 48 h, 72 h, 96 h, 120 h, 168 h and 216 hours post-dose.
  • isotretinoin 16 mg isotretinoin 16 stearoyl macrogol glycerides (Gelurire 50/13 ®) 192 soya bean oil refined 104 sorbitane oleate (Span 80 ®) 16
  • the dose of 16 mg of the formulation corresponding to the present invention gives a bioavailability similar to 20 mg of the marketed formulation, what is the evidence of the supra-bioavailability of the formulation corresponding to the present invention.

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Abstract

An oral pharmaceutical composition of isotretinoin containing at least two lipidic excipients, one of them being hydrophilic (i.e. having an HLB value superior or equal to 10), the other being an oily vehicle

Description

  • The present invention relates to an oral pharmaceutical composition of isotretinoin containing at least two excipients, one of them being hydrophilic (i.e. having an HLB value superior or equal to 10), the other being an oily vehicle.
    • THE PRIOR ART
  • Isotretinoin (13-cis retinoic acid or 13-cis vitamin A), its isomers and some of its analogs are widely known to have a therapeutical activity in the treatment of several severe skin disorders like cystic acne, hypertrophic lupus erythematosus, keratinization disorders. Some evidences have also been brought about the activity of isotretinoin in basal cell carcinoma and squamous cell carcinoma.
  • Unfortunately, isotretinoin is also a highly toxic drug. Indeed, although isotretinoin, which is a cis derivative, is known to be less toxic than all trans vitamin A derivatives, side effects resulting from its use such as headache, vomiting, irritation of mucosa and liver toxicity, occur frequently. Furthermore, isotretinoin is known to be highly teratogenic in both animals and humans.
  • In order to well understand the interest of this invention, it is important to briefly summarize the physico-chemical pharmacokinetic properties.
  • Isotretinoin is a reddish-orange powder. It is decomposed in presence of light and atmospheric oxygen. Isotretinoin is very poorly soluble in water what made its bioavailability quite low after an oral intake (25% in fasted conditions and 40% in fed conditions). The maximum concentration (Cmax) is reached after 2-4 hours, while the (Cmax) of the active metabolite, 4-oxo-isotretinoin is reached after 6 hours. The elimination half-life of isotretinoin is of 7 to 37 hours while the half life (t1/2) of the active metabolite is of 11 to 50 hours. The steady-state concentrations of isotretinoin are reached after 1 week of treatment.
  • Very few publications and/or patents about the pharmaceutical formulation of isotretinoin are available. The drug is available on most markets under the form of a soft gelatine capsule containing a fatty liquid formulation of isotretinoin.
  • The U.S. Pat. No. 4,464,394 describing for the first time the therapeutical use of isotretinoin also describes briefly some possibilities of compositions including it. It involves the use of one antioxidant agent and of one carrier like lactose, starches or polyethyleneglycols.
  • The EP patent 0184942 describes more specific compositions of isotretinoin involving the use of one antioxidant, one chelating agent, one pharmaceutical carrier and one suspending agent. The composition obtained is stable during time.
  • The U.S. Pat. No. 4,545,977 relates to improved compositions of isotretinoin wherein taurine is associated with isotretinoin to reduce the side effects thereof.
  • The U.S. Pat. No. 5,716,928 describes a method for increasing bioavailability and for reducing inter and intra individual variability of an orally administered hydrophobic pharmaceutical compound, which comprises orally administering the pharmaceutical compound with an essential oil or essential oil component in an amount sufficient to provide greater bioavailability of the active ingredient.
  • The U.S. Pat. No. 6,028,054 relates to a method for increasing bioavailability of an orally administered hydrophobic pharmaceutical compound to human, which comprises orally administering the pharmaceutical compound concurrently with a bioenhancer comprising an inhibitor of e-cytochrome P450 3A enzyme or an inhibitor of P-glycoprotein mediated membrane transport.
  • The U.S. Pat. No. 5,993,858 describes a self microemulsifying excipient formulation for increasing the bioavailability of a drug which includes an emulsion including an oil or other lipid material, a surfactant and an hydrophilic co-surfactant.
  • What is not described is a composition of isotretinoin containing at least two lipid materials, one of them being hydrophilic. The said composition may be a suspension, emulsion or microemulsion.
    • BRIEF DESCRIPTION OF THE INVENTION
  • The advent of high throughput combinatorial chemistry and efficient receptor based in vitro activity screen has resulted in molecules with poor physicochemical (ex: dissolution) properties for absorption across the gastro-intestinal tract, like isotretinoin.
  • It is increasingly being recognized by the pharmaceutical industry that for these molecules drug delivery systems play an important role for improving oral bioavailability.
  • Although the process of passive diffusion is responsible for absorption of non ionized lipophilic molecules via the transcellular pathway, specialized absorption mechanisms, first-pass metabolisms and efflux systems at the gastrointestinal wall appear to play a major role for lack of absorption and poor bioavailability for some molecules.
  • Isotretinoin is characterized by a low absolute bioavailability and a high inter and intra individual variability. Isotretinoin also presents a wide range of side effects among which some are severe (ocular, skin anemia, hepatic, . . . ). It is consequently of a particular interest to dispose of a reliable, stable and highly bioavailable formulation of isotretinoin.
  • Several possibilities are available to the formulator to increase the bioavailability of active ingredients (Table A).
  • TABLE A
    I. Use of salts, polymorphs. Precursors of the active molecule
    (=prodrugs)
    II. Reduction of the particles' site of the active principle and of the
    excipients used (by trituration, grinding, micronization,
    precipitation controlled by solvent, temperature or ultrasonics).
    III. Solid dispersions:
    Eutectic mixes
    Solid solutions
    Vitreous solutions
    IV. Recrystallization in an aqueous solution of a surfactant
    V. Modification of the microenvironment:
    Hydrophilization
    pH (acidification)
    VI. Incorporation of the active principle to lipidic systems
  • It has been found that a semi-solid dosage form containing isotretinoin was advantageous for obtaining a good bioavailability of the isotretinoin. A semi-solid dosage form containing isotretinoin is a form in which isotretoin is mixed with suitable melted excipients. The molten mix is then filled for example into hard gelatine capsules or other pharmaceutically acceptable capsules. At ambient temperature (temperature for example of less than 20° C.), the content of the capsule is solid while at temperature higher than 20° C. (for example at temperature greater or equal to 30° C., advantageously greater or equal to 35° C., preferably substantially at body temperature+/−37° C.), it is liquid or semi-solid (paste). The isotretinoin may be solubilized in the mix of excipients or partially solubilized. The active ingredient may also be formulated as a suspension, emulsion or microemulsion. Various lipidic excipients are available to the formulator to obtain a semi-solid formulation. Excipients compatible with hard gelatin capsule shells are: lipophilic liquid vehicles (refined specialty oils, medium-chain triglycerides and related esters), semi-solid lipophilic vehicles, solubilizing agents, emulsifying agents and absorption enhancers. The classification of fatty excipients is based on the hydrophilicity or lipophilicity of the excipients, characterized by the hydrophilic/lipophilic balance value (HLB). Examples of lipophilic excipients are vegetable oils (peanut oil, olive oil, soyabean oil, . . . ), fatty acids (stearic acid, palmitic acid, . . . ), fatty alcohols, . . . Examples of hydrophilic excipients are polyethyleneglycol (PEG) with a molecular weight superior to 3,000. Examples of amphiphilic (=presenting lipophilic and hydrophilic properties) excipients are Poloxamers, Lecithin, PEG esters (Gelucire®), . . . .
  • The advantages of the semi-solid formulations of the invention are multiple for isotretinoin: protection of the active ingredient from air and humidity, possibility of increasing the dissolution rate of the molecule and hence of the bioavailability, diminution of the risk of contamination of the operator, diminution of the risk of cross contamination, no possibility of demixing under the effect of vibrational mixing during manufacturing process, facility of the production process. The choice of the nature of the formulation of course influenced the stability of the pharmaceutical form and the bioavailability of the isotretoin contained in it. Generally, a maximum bioavailability is achieved by preparing and keeping the drug in the amorphous/solubilized state in a solid dispersion or in a lipid-based formulation. For these systems, the barrier we are avoiding is the compound a washing-out a of solution to a large extent into a insoluble crystalline form during the dissolution/release step in vivo.
  • These systems may consist of suspension, emulsion, microemulsion, self-emulsifying drug delivery systems (SEDDS®) or self-emulsifying microemulsion drug delivery system (SMEDDS®).
  • Microemulsions have the added advantage over suspensions such as emulsions and dispersions since thermodynamically they are more stable, that they can be manufactured with little energy input and have generally a longer shelf-life. Nevertheless, a microemulsion formulation is not a guarantee of higher bioavailability in comparison to suspension a described hereafter.
  • The formation of oil-in-water (O/W) and water-in-oil (W/O) microemulsions usually involves a combination of 3-5 basic compounds i.e. oil, surfactant, cosurfactant, water and electrolytes. The challenge is to select for a particular application oil(s) and surfactant(s) that are acceptable from a toxicological perspective and that allow to obtain a high bioavailability of the drug, i.e isotretoin.
  • The assessment of the quality of semi-solid lipid based formulations is quite difficult since the in vitro dissolution test is of little help. Indeed, the in vitro/in vivo correlation between dissolution and bioavailability is very poor for this kind of formulations. Other analytical tools are available to the formulator to try to predict the in vivo bioavailability of isotretinoin from various formulations like CACO-2 cells model, the assessment of the percentage of drug dissolved in the formulation, differential scanning calorimetry, microscopy, . . . .
  • Nevertheless, none of them present a guarantee of in vitro/in vivo correlation and ultimately only pharmacokinetic studies on human subjects are reliable to assess the bioavailabiltiy of the drug.
    • DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
  • The pharmaceutical composition of the invention is an oral semi-solid pharmaceutical composition of isotretinoin containing two lipidic excipients, one of them being hydrophilic i.e. having a HLB value of at least 10, for example equal to 10, but preferably greater than 10, such as greater or equal to 12, for example comprised between 12 and 14, and the other being an oily vehicle.
  • The pharmaceutical composition of the invention contains advantageously at least one hydrophilic excipient with a HLB value of at least 10 selected from the group consisting of glyceroyl macrogoiglycerides, polyethyleneglycol derivatives, and mixtures thereof. Preferably, the pharmaceutical composition contains from 20 to 80% by weight of hydrophilic excipient with a HLB value of at least 10 selected from the group consisting of glyceroyl macrogolglycerides, polyethyleneglycol derivatives, and mixtures thereof.
  • The oily vehicle is selected from the group consisting of vegetable oils, medium chain triglycerides, fatty acid esters, amphiphilic oil, glycerol oleate derivative, and mixtures thereof. For example, the composition contains from 5 to 70% by weight of an oily vehicle selected from the group consisting of vegetable oils, medium chain triglycerides, fatty acid esters, amphiphilic oil, glycerol oleate derivative, and mixtures thereof.
  • According to another detail of preferred pharmaceutical compositions of the invention, the composition further contains at least one surfactant, preferably selected from the group consisting of sorbitan fatty acid esters, polysorbate derivatives, polyoxyethylene sorbitan fatty acid esters, sodium laurylsulphate, derivatives of lecithine, propylene glycol esters, fatty acid esters of propylene glycol, fatty acid esters of glycerol, polyethylene glycol, and mixtures thereof. For example, the composition contains from 1 to 10% by weight of at least one surfactant.
  • Furthermore, the pharmaceutical formulation of the invention contains advantageously at least one disintegrant, preferably selected from the group consisting of povidone derivative, sodium croscarmellose and mixtures thereof.
  • The pharmaceutical composition of the invention may contain one or more surfactants and/or one or more disintegrants, but contains preferably one or more compounds acting as surfactants and one or more compounds acting as disintegrants.
  • The invention relates also to a pharmaceutical acceptable capsule containing at least one semi-solid composition of the invention, for example at least one composition of the invention as disclosed hereabove. The capsule is for example selected from the group consisting of hard gelatine capsules, soft gelatine capsules, hypromellose capsules, starch capsules.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a ternary diagram of a formulation containing only Gelucire® 50/13 and soyabean oil, the third component being water;
  • FIG. 2 shows the dissolution rate of a reference product (Roaccutane®-20 mg active agent), of a suspension containing 20 mg Isotretoin and of an emulsion SEDDS® containing 10 mg Isotretoin;
  • FIG. 3 shows an in vivo comparative pharmacokinetic profile of isotretinoin;
  • FIG. 4 gives the comparative pharmacokinetic profile of different formulations for isotretinoin,
  • FIG. 5 gives the comparative pharmacokinetic profile of different formulations for 4-oxo-isotretinoin, the active metabolite of isotretinoin and
  • FIGS. 6 and 7 describe the mean pharmacokinetic profile of isotretinoin and 4-oxoisotretinoin for two formulations.
    •  DESCRIPTION OF EXAMPLES
  • The present invention relates thus to a semi-solid formulation of isotretinoin containing at least 2 lipidic excipients, one of them being an hydrophilic excipient (having a high HLB value namely >10) and the other an oily excipient. The molten mix of these two excipients allows to totally or partially (depending on the ratio between excipients) dissolve isotretinoin. Different kinds of formulations (SEDDS® or suspensions) of isotretinoin have been formulated. For suspensions, it was possible to dissolve a high fraction of isotretinoin in the mix of excipients and even the whole quantity of the active ingredient if the manufacturing conditions (high temperature and long time of mixing) and the formulations were optimized. Excipients particularly suitable for the dissolution of isotretinoin were lauroyl Macrogol-32 glycerides (Gelucire® 44/14, Gattefossé) and Stearoyl Macrogol-32 glycerides (Gelucire® 50/13, Gattefossé). When those hydrophilic components are melted together with an oily vehicle, it allows to obtain very stable suspensions of isotretinoin in which an important part of the active ingredient is dissolved. A surfactant may also be added to the formulation to still improve the physical stability of the suspension.
  • SEDDS® formulations of isotretinoin are also stable and may give an improved bioavailability of the drug.
  • Ternary diagrams allow to observe different areas corresponding to different physical states namely coarse emulsion, true emulsion, lamellar solution or micellar solution when the ratio between excipients changes.
  • The behaviour of the formulation in presence of water changes when the ratio changes. One example of this ternary diagram is given in FIG. 1 for a formulation of isotretinoin containing Gelucire® 50/13 and soyabean oil.
    • EXAMPLES Example 1 Effect of Different Lipophilic Compounds
  • The effect of different lipophilic excipients was evaluated in the form of semi-solid capsules. The semi-solid capsules were made by addition of the active substance at the pre-melted lipophilic compounds followed by the filling of the liquid into hard gelatin capsule.
  • The active substance was incorporated into formulations, listed in table I, consisting of glyceroyl macrogolglyceride associated with soyabean oil or derivative, medium chain triglyceride.
  • TABLE I
    Formulation no
    (mg) 1 2 3 4 5
    Isotretinoin 20 20 20 20 20
    Labrafil ® M1944 CS 132
    Gelucire ® 50/02 198 93
    Gelucire ® 44/14 217
    Gelucire ® 50/13 76 60 60
    Soya bean oil 304 320
    Mygliol ® 320
  • The use of stearoyl macroglyceride (Gélucire® 50/13, Gattefosse) and soyabean oil allows to obtain a formulation with a dissolution profile similar to the reference (Roaccutane® 20 mg, Roche).
  • The formulation with labrafil or Gelucire® 50/02 are too lipophilic to give a good dissolution in water.
  • In general, the use of an oily excipient can improve the absorption of lipophilic drug by increasing the solubility of the drug in the lipidic phase, but the release of the active ingredient from the formulation can be slowed down due to the high affinity of the drug for the oily phase.
  • The use of dispersed systems (emulsions or suspensions) instead of only lipophilic or hydrophilic vehicles, improves the absorption of the drug as well as increasing a larger contact surface.
  • Concerning the Gelucire®, the process of drug release varies according to the HLB of the excipient. Gelucire® with high HLB values were found to be the most favorable for a rapid release of the drug (by diffusion and erosion).
  • The drug release profiles of the formulations 1 to 5 were evaluated in phosphate buffer pH 7.5 with laurylsulfate and pancreatin. The percent of isotretinoin released after 4 hours is given in the following table II.
  • TABLE II
    percent of isotretinoin released after 4 hours
    Formulations n
    o
    1 2 3 4 5
    % released 20.1 69.1 46.0 60.3 78.1
  • The percent of isotretinoin released from the reference (Roaccutane® 20 mg) after 4 hours is 55.37%
    • Example 2 Influence of the Ratio Oily Vehicle/Surfactive Agent on the Dissolution and Absorption of the Formulation
  • The study of the ratio oily vehicle/surfactive agent with the construction of a ternary diagram gives information on the dissolution profile of the formulation in water.
  • Stearoyl macrogolglyceride (Gelucire® 50/13) known as a drug solubilizer and emulsifying agent of different drugs (in SMEDDS® or SEDDS®) was tested in association with soyabean oil.
  • This component has the ability to solubilize a great part of isotretinoin in the formulation.
  • This is listed in table III
  • TABLE III
    Formulations n°
    1 2 3 4 5 6
    (mg)
    Isotretinoin 20 10 10 20 20 20
    Soyabean oil 270 135 40 152 57 133
    Gelucire ® 50/13 84 42 200 228 323 247
    Filling weight 374 187 260 400 400 400
    Ratio oil/ 3.2 3.2 0.2 0.67 0.17 0.54
    Gelucire ® 50/13
  • In the presence of water, the behaviour of these formulations are different
      • formulations 1 and 2: formation of coarse emulsion with large droplet sizes
      • formulations 3 and 5: formation of micellar phase or microemulsion
      • formulations 4 and 6: formation of emulsion with homogeneous droplet size
  • The percentage of isotretinoin released increases generally with the percentage of Gelucire® in the formulation (increased solubility of the active in this vehicle). For the formulation 1 (ratio oil/Gelucire® 50/13=3.2) 54.9% released after 4 hours and for the formulation 3 (ratio oil/Gelucire® 50/13:0.2), 91.2% released after 4 hours.
    • Dissolution Test
  • For poorly soluble molecules, the prediction power of the in vitro dissolution test is weak since the in vitro/in vivo correlation is known to be poor. Nevertheless, an optimized dissolution test (using enzymes and surfactant) is of some help to assess the rate of release of the drug from the lipidic composition. It must be noted that the conditions of the dissolution (dissolution medium, speed of the paddles, temperature . . . ) test influence dramatically the results of the test and should consequently be standardized to allow comparison between various formulations.
  • The conditions of the solution test used for assessing the dissolution of isotretinoin were the following:
      • paddle apparatus
      • 150 rpm
      • 37° C.
      • buffer pH 7.5 with laurylsulfate 2.5% and pancreatin 1 g/L
  • FIG. 2 shows the dissolution rate of a reference product (Roaccutane®-20 mg active agent), of a suspension containing 20 mg Isotretoin and of an emulsion SEDDS®containing 10 mg Isotretoin (formulation given hereinbelow).
  • As the information brought by the dissolution test is poor in term of correlation with in vivo bioavailability, it is of interest to dispose of other means to predict the in vivo bioavailability.
  • The caco-2 cell culture system can be used for determining permeability of compounds (especially for poorly soluble compounds). The caco-2 cell model allows to measure the transport of drug from the apical to the serosal side as well as from the serosal to the apical side. This allows to determine if an efflux system is operational.
  • The caco-2 cells model is interesting because:
      • The cells used are from human origin (contrary to the models using segments of animal's guts). They are coming from an adenocarcinoma of the human colon but spontaneously differentiate into small intestine's epithelial cells. When put in culture, they form a monolayer of polarized cells expressing several enzymatic systems.
      • It offers a better prediction of the human intestine absorption than the animals models
      • The reproducibility of the test is relatively high
      • It allows to take samples from both apical and basolateral sides
  • Caco-2 cells experiments have been performed with one SEDDS® and one suspension isotretinoin formulations.
    • Results
  • It was first proven that neither the active ingredient nor the excipient used in the formulations were toxic for the cells. It was also proven that the integrity of the membranes of the cells was maintained during the whole experience.
    • Methodology:
  • The formulations tested are put in solution in 250 ml of BME. Taurocholate (10 mM) was added to the solutions to better mimate the in physiological conditions. The different solutions so prepared are put in contact with Caco-2 cells at the apical or basolateral side. The cells culture inserts) are incubated for 3 hours at 37° C. and samples of 100 μl are taken every hours
  • The formulations tested were the following:
  • Formulation SEDDS® (Batch Number 26F97/1):
  • Isotretinoin: 10 mg
  • Gelucire® 50/13: 134 mg
  • Phospholipon 90®: 11 mg
  • Tween 80®: 71 mg
  • IPP®: 24 mg
  • Pro capsula una
  • Formulation Suspension (Batch Number 25F97/1)
  • Isotretinoin: 20 mg
  • Gelucire® 50/13: 83.7 mg
  • Soyabean oil: 270 mg
  • Procapsula una
    • Results
  • Passage of Formulations from Apical Side→Basolateral Side
  • Time SEDDS ® Suspension SEDDS ® + Suspension +
    minutes (26F97/1) (25F97/1) TC TC control
    60 0.7721 0.6708 0.7019 0.6469 0.0718
    120 2.4096 0.8749 1.4347 0.9513 0.1836
    180 2.6226 1.1311 3.2419 1.5073 0.6156
  • Passage of Formulations from Basolateral Side→Apical Side
  • Time SEDDS ® Suspension SEDDS ® + Suspension +
    minutes (26F97/1) (25F97/1) TC TC control
    60 2.0496 0.3948 8.1291 0.8713 0.0650
    120 3.0844 0.9068 8.3496 1.8460 0.1131
    180 4.3653 1.0763 9.7110 2.0779 0.1481
  • The results demonstrate that the passage of isotretinoin is superior for the SEDDS®formulation than for the suspension formulation. In order to confirm these results, a comparative pharmacokinetics study has been performed.
    • PK Studies
  • The bioavailability of SEDDS® (26F97/1) and suspension (25F97/1) isotretinoin formulations has been assessed and compared to the bioavailability of the reference (Roaccutane® 20 mg, Hoffman LaRoche) on six healthy volunteers in a single dose, three way, cross-over pharmacokinetic study). The drug was taken with food (standardized breakfast). The plasma concentration of isotretinoin and its active metabolite 4-oxo-isotretinoin were quantified using a fully validated LC/MS/MS method.
  • The FIG. 3 described the mean pharmacokinetic profile obtained for each formulation.
  • The following table gives the value of the main pharmacokinetics parameters obtained for each formulation of isotretinoin.
  • AUC72 h Cmax Tmax
    Formulations (ng · h/ml) (ng/ml) (h)
    Roaccutane ® 20 mg 1747.89 116.63 1.83
    (96C15315AA)
    Suspension 20 mg 4308.72 230.96 5.67
    (25F97/1)
    SEDDS ® 10 mg 1494.64 98.36 3.00
    (26F97/1)
  • It appears that both the SEDDS® and the suspension formulation are able to significantly increase the bioavailability of isotretinoin in comparison to the marketed reference. Indeed the ratio between AUC72h of the suspension 20 mg and Roaccutane® 20 mg is of 2.47. The SEDDS® 10 mg present an AUC72h similar to this of Roaccutane® 20 mg what means an approximately 2-fold increase of bioavailability (ratio AUC72h SEDDS®10 mg/AUC72h Roaccutane® 20 mg=0.86). Furthermore, the suspension and SEDDS® formulations both presented a lower intraindividual variability of the bioavailability as demonstrated by the values of relative standard deviations (rsd) which are of 36.0%, 22.72% and 28.18% for Roaccutane® 20 mg, suspension 20 mg and SEDDS® 10 mg respectively.
  • Nevertheless, the results obtained in vivo are not correlated with the results obtained on caco-2 cells since on this model the permeability of the SEDDS® formulation was much higher than the permeability of the suspension formulation while in vivo the suspension formulation gives the best results.
  • A second pharmacokinetic study was performed on completely different formulations (6 subjects, 2-way, fed, cross-over study). Those were formulations of isotretinoin under the form of a suspension in which the ratio between Gelucire® 50/13 and soyabean oil was very different that the previous formulation of suspension
  • The two formulations tested were the following:
  • F1: suspension without surfactant (batch number H23K99/1)
  • Isotretinoin: 20 mg
  • Gelucire® 50/13: 247 mg
  • Soyabean oil: 133 mg
  • F2: suspension with surfactant (batch number H07L99/1)
  • Isotretinoin: 20 mg
  • Gelucire® 50/13: 240 mg
  • Soyabean oil: 130 mg
  • Span 80®: 20 mg
  • The FIG. 4 gives the comparative pharmacokinetic profile of each formulation for isotretinoin
  • The FIG. 5 gives the comparative pharmacokinetic profile of each formulation for 4-oxo-isotretinoin, the active metabolite of isotretinoin.
  • in order to confirm the first bioavailability data obtained with the present invention, a larger pharmacokinetic study has been performed.
  • The bioavailability of a capsule of isotretinoin 16 mg (see the formulation herebelow) from the present invention has been assessed and compared to the bioavailability of the reference (ROACCUTANE® 20 mg capsule, Roche) on 24 healthy subjects.
  • This study (SMB-ISO-SD011) was a single dose, two treatment, two period, two sequence, randomised, crossover and with at least 18 days wash-out between the two periods.
  • The subjects were healthy caucasian volunteers of both sexes (non-pregnant, non-breast-feeding), aged 18 to 50 years, non smokers or smoking less than 10 cigarettes per day.
  • The drugs was taken with food (a standardized breakfast).
  • Blood samples were collected according to the following sampling schedule: pre-dose and 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 10 h, 12 h, 14 h, 24 h, 36 h, 48 h, 72 h, 96 h, 120 h, 168 h and 216 hours post-dose.
  • The plasma concentration of isotretinoin and its active metabolite 4-oxo-isotretinoin were quantified using a fully validated LC/MS/MS method. The continuous variables were evaluated according to an univariate ANOVA, based on log-transformed data. The Wilcoxon non-parametric ANOVA were used where appropriate. Bioequivalence was evaluated using the Shuirman two one-sided t-test (90% CI) and the westlake single sided confidence interval (95% CL)
  • The FIGS. 6 and 7 describe the mean pharmacokinetic profile of isotretinoin and 4-oxoisotretinoin for the two formulations (n=24 subjects) while the tables herebelow give the comparative main pharmacokinetic parameters.
  • Formulation of isotretinoin 16 mg (mg/capsule)
    isotretinoin 16
    stearoyl macrogol glycerides (Gelurire 50/13 ®) 192
    soya bean oil refined 104
    sorbitane oleate (Span 80 ®) 16
  • As seen, the dose of 16 mg of the formulation corresponding to the present invention gives a bioavailability similar to 20 mg of the marketed formulation, what is the evidence of the supra-bioavailability of the formulation corresponding to the present invention.
  • The tables hereinbelow gives the value of the main pharmacokinetics results and statistical analysis obtained for each formulation of isotretinoin and 4-oxoisotretinoin.
  • This study demonstrated that ROACCUTANE® 20 mg and isotretinoin 16 mg x are bioequivalent after a single oral dose administration of each product in fed conditions. Indeed, the primary parameters AUC (AUC∞ and AUC216h) were within the predetermined confidence interval.
  • This study demonstrated also that Isotretinoin 16 mg has a safety profile comparable with that described in the literature for other isotretinoin preparations and similar to this of ROACCUTANE® 20 mg.
  • Pharmacokinetic results and statistical analysis of comparative study in 24 volunteers for isotretinoin (log-transformed data)
  • Bioequivalence tests
    Results Shuirman
    ROACCUTANE ® 90% CI Westlake
    Parameter
    20 mg Isotretinoin 16 mg Range 95% CL
    AUC∞ 5657.09 (ng · h/ml) 5696.92 (ng · h/ml) 92-123 19.07
    ±SD ±2682.98 ±1938.89
    ±RSD ±47.42 ±34.03
    AUC216 h 5601.36 (ng · h/ml) 5664.39 (ng · h/ml) 92-124 19.51
    ±SD ±2670.85 ±1953.52
    ±RSD ±47.68 ±34.48
    Cmax 386.68 (ng/ml) 441.79 (ng/ml) 103-140  28.81
    ±SD ±218.21 ±197.43
    ±RSD ±56.43 ±44.68
    Tmax 4.92 (h) 4.50 (h) / /
    ±SD ±2.22 ±0.66
    ±RSD ±45.24 ±14.65
  • Pharmacokinetic results and statistical analysis of comparative study in 24 volunteers for 4-oxoisotretinoin (log-transformed data)
  • Bioequivalence tests
    Results Shuirman
    ROACCUTANE ® 90% CI Westlake
    Parameter
    20 mg Isotretinoin 16 mg Range 95% CL
    AUC∞ 5750.36 (ng · h/ml) 5769.04 (ng · h/ml) 92-124 19.65
    ±SD ±2717.38 ±2161.97
    ±RSD ±47.26 ±37.48
    AUC216 h 5638.32 (ng · h/ml) 5712.21 (ng · h/ml) 92-125 20.46
    ±SD ±2704.73 ±2126.61
    ±RSD ±47.80 ±37.23
    Cmax 111.52 (ng/ml) 115.15 (ng/ml) 94-125 20.18
    ±SD ±69.62 ±66.25
    ±RSD ±62.43 ±57.53
    Tmax 17.83 (h) 16.33 (h) / /
    ±SD ±10.60 ±10.11
    ±RSD ±59.43 ±61.88

Claims (38)

1-13. (canceled)
14. A low dose oral pharmaceutical composition of isotretinoin comprising about 16 mg of isotretinoin, wherein the composition exhibits bioequivalence to a 20 mg formulation of Roaccutane upon administration to a human subject, wherein the bioequivalence is established by a 90% confidence interval for AUC0-∞ which is between 80% and 125% upon administration with a continental breakfast.
15. The low dose oral pharmaceutical composition of claim 14, wherein the composition further comprises at least a first and a second lipidic excipient, wherein the first lipidic excipient has a HLB value equal to or greater than 10.
16. The low dose oral pharmaceutical composition of claim 15, wherein the first lipidic excipient is selected from the group consisting of glyceroyl macrogolglycerides, polyethylene glycol esters, and mixtures thereof.
17. The low dose oral pharmaceutical composition of claim 15, wherein the second lipidic excipient is selected from the group consisting of vegetable oils, medium chain triglycerides, fatty acid esters, glycerol oleate and mixtures thereof.
18. The low dose oral pharmaceutical composition of claim 15, wherein the first lipidic excipient comprises between 20% to 80% w/w of the composition and the second lipidic excipient comprises between 5% to 70% w/w of the composition.
19. The low dose oral pharmaceutical composition of claim 15, wherein the first lipidic excipient has a HLB value of at least 12.
20. The low dose oral pharmaceutical composition of claim 15, wherein the first lipidic excipient has a HLB value of at least 13.
21. The low dose oral pharmaceutical composition of claim 14, wherein the composition comprises a semi-solid partly in suspension and partly in solution of isotretinoin.
22. The low dose oral pharmaceutical composition of claim 21, wherein the composition comprises a semi-solid suspension of isotretinoin.
23. The low dose oral pharmaceutical composition of claim 21, wherein the composition comprises a semi-solid solution of isotretinoin.
24. The low dose oral pharmaceutical composition of claim 15, which further comprises at least one surfactant.
25. The low dose oral pharmaceutical composition of claim 24, wherein the surfactant is selected from the group consisting of sorbitan fatty acid esters, polysorbate compounds, polyoxyethylene sorbitan fatty acids esters, sodium lauryl sulphate, compounds of lecithin, propylene glycol esters, fatty acid esters of propylene glycol, fatty acid esters of glycerol, and mixtures thereof.
26. The low dose oral pharmaceutical composition of claim 24, wherein the surfactant comprises between 1% to 10% w/w of the composition.
27. The low dose oral pharmaceutical composition of claim 15, which further comprises at least one disintegrant.
28. The low dose oral pharmaceutical composition of claim 27, wherein the disintegrant is selected from the group consisting of crosspovidone, sodium croscarmellose, and mixtures thereof.
29. The low dose oral pharmaceutical composition of claim 14, wherein the composition comprises from about 10 mg to 20 mg of isotretinoin.
30. The low dose oral pharmaceutical composition of claim 29, wherein the composition comprises from about 16 mg to 20 mg of isotretinoin.
31. The low dose oral pharmaceutical composition of claim 30, wherein the composition comprises 16 mg of isotretinoin.
32. The low dose oral pharmaceutical composition of claim 14, wherein the composition is in the form of a capsule.
33. The low dose oral pharmaceutical composition of claim 14, wherein the composition is in the form of a capsule.
34. An oral pharmaceutical composition of isotretinoin, wherein the composition exhibits an AUC0-∞ 90% confidence interval comprised between 96% and 150% when compared to the same dosage strength of isotretinoin from Roaccutane after administration with a continental breakfast.
35. The oral pharmaceutical composition of claim 34, wherein the composition further comprises at least a first and a second lipidic excipient, wherein the first lipidic excipient has a HLB value equal to or greater than 10.
36. The oral pharmaceutical composition of claim 31, wherein the first lipidic excipient is selected from the group consisting of glyceroyl macrogolglycerides, polyethylene glycol esters, and mixtures thereof.
37. The oral pharmaceutical composition of claim 31, wherein the second lipidic excipient is selected from the group consisting of vegetable oils, medium chain triglycerides, fatty acid esters, glycerol oleate and mixtures thereof.
38. The oral pharmaceutical composition of claim 31, wherein the first lipidic excipient comprises between 20% to 80% w/w of the composition and the second lipidic excipient comprises between 5% to 70% w/w of the composition.
39. The oral pharmaceutical composition of claim 31, wherein the first lipidic excipient has a HLB value of at least 12.
40. The oral pharmaceutical composition of claim 31, wherein the first lipidic excipient has a HLB value of at least 13.
41. The oral pharmaceutical composition of claim 34, wherein the composition comprises a semi-solid partly in suspension and partly in solution of isotretinoin.
42. The oral pharmaceutical composition of claim 41, wherein the composition comprises a semi-solid suspension of isotretinoin.
43. The oral pharmaceutical composition of claim 41, wherein the composition comprises a semi-solid solution of isotretinoin.
44. The oral pharmaceutical composition of claim 35, which further comprises at least one surfactant.
45. The oral pharmaceutical composition of claim 44, wherein the surfactant is selected from the group consisting of sorbitan fatty acid esters, polysorbate compounds, polyoxyethylene sorbitan fatty acids esters, sodium lauryl sulphate, compounds of lecithin, propylene glycol esters, fatty acid esters of propylene glycol, fatty acid esters of glycerol, and mixtures thereof.
46. The oral pharmaceutical composition of claim 44, wherein the surfactant comprises between 1% to 10% w/w of the composition.
47. The oral pharmaceutical composition of claim 35, which further comprises at least one disintegrant.
48. The oral pharmaceutical composition of claim 45, wherein the disintegrant is selected from the group consisting of crosspovidone, sodium croscarmellose, and mixtures thereof.
49. The oral pharmaceutical composition of claim 34, wherein the composition comprises from about 10 mg to 20 mg of isotretinoin.
50. The oral pharmaceutical composition of claim 56, wherein the composition is in the form of a capsule.
US13/713,897 2000-09-22 2012-12-13 Pharmaceutical semi-solid composition of isotretinoin Expired - Lifetime US9089534B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US13/713,897 US9089534B2 (en) 2000-09-22 2012-12-13 Pharmaceutical semi-solid composition of isotretinoin
CA2836228A CA2836228A1 (en) 2012-12-13 2013-12-13 Pharmaceutical semi-solid composition of isotretinoin
BR102013032172-9A BR102013032172A2 (en) 2000-09-22 2013-12-13 PHARMACEUTICAL SEMICONDUCTOR COMPOSITION OF ISOTRETINOIN
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015094574A1 (en) * 2013-12-18 2015-06-25 Galephar Pharmaceutical Research, Inc. Pharmaceutical semi-solid composition of isotretinoin

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000075365A2 (en) 1999-06-08 2000-12-14 University Of Iowa Research Foundation Compounds and methods to enhance raav transduction
CA2423170A1 (en) 2000-09-22 2002-03-28 Galephar M/F Pharmaceutical semi-solid composition of isotretinoin
ITMI20011338A1 (en) 2001-06-26 2002-12-26 Farmatron Ltd ORAL PHARMACEUTICAL COMPOSITIONS WITH IMMEDIATE RELEASE OF THE ACTIVE INGREDIENT
FI20030426A (en) * 2003-03-24 2004-09-25 Tomi Jaervinen cyclodextrin complexes
JP2007524379A (en) 2003-03-31 2007-08-30 ユニバーシテイ・オブ・アイオワ・リサーチ・フアウンデーシヨン Pharmaco-gene therapy for epithelial sodium channel related disorders
SE0303135D0 (en) * 2003-11-25 2003-11-25 Lipocore Holding Ab Controlled food effect composition
HUE029192T2 (en) * 2005-03-21 2017-02-28 Teva Czech Ind S R O Crystallization inhibitor and its use in gelatin capsules
EP2123255B1 (en) * 2007-02-16 2013-05-15 ASKA Pharmaceutical Co., Ltd. Pharmaceutical composition containing fine particle oil-based suspension
WO2010109259A1 (en) * 2009-03-26 2010-09-30 Grufarcol Ltda Method for preparing soft gel formulations of liquid isotretinoin and formulations obtained
EP2432553A2 (en) 2009-05-20 2012-03-28 Ranbaxy Laboratories Limited Liquid dosage forms of isotretinoin
BRPI1010972A2 (en) 2009-05-20 2019-04-16 Ranbaxy Laboratories Limited topical composition in the form of a solution and method for treating acne or other skin related disorders
US10022348B2 (en) 2009-05-20 2018-07-17 Sun Pharmaceutical Industries Limited Topical solution of isotretinoin
JP2016535106A (en) 2013-09-25 2016-11-10 スリーエム イノベイティブ プロパティズ カンパニー Composition for electric field grading
ES2680444T3 (en) * 2014-01-17 2018-09-07 Oncoral Pharma Aps Solid oral dosage form of irinotecan for cancer treatment
AU2015265454A1 (en) 2014-05-29 2016-12-15 Sun Pharmaceutical Industries Limited Oral pharmaceutical composition of isotretinoin
MX2016015464A (en) * 2014-06-02 2017-03-27 Sun Pharmaceutical Ind Ltd Oral pharmaceutical composition of isotretinoin.
JP2017521470A (en) 2014-07-31 2017-08-03 サン ファーマシューティカル インダストリーズ リミテッドＳｕｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌ Ｉｎｄｕｓｔｒｉｅｓ Ｌｔｄ． Oral pharmaceutical composition of isotretinoin
US9750711B2 (en) 2014-10-01 2017-09-05 Sun Pharmaceutical Industries Limited Low dose oral pharmaceutical composition of isotretinoin
MA40781A (en) * 2014-10-01 2017-08-08 Sun Pharmaceutical Ind Ltd PHARMACEUTICAL COMPOSITION OF LOW DOSAGE ISOTRETINOIN FOR ORAL USE
MX2017015137A (en) * 2015-05-25 2018-03-28 Sun Pharmaceutical Ind Ltd Once daily oral pharmaceutical composition of isotretinoin.
CA2987517A1 (en) * 2015-05-29 2016-12-08 Sun Pharmaceutical Industries Limited Oral pharmaceutical composition of isotretinoin
WO2017139381A1 (en) 2016-02-08 2017-08-17 University Of Iowa Research Foundation Methods to produce chimeric adeno-associated virus/bocavirus parvovirus
AU2017229347A1 (en) 2016-03-07 2018-11-01 University Of Iowa Research Foundation AAV-mediated expression using a synthetic promoter and enhancer
US9949967B2 (en) 2016-04-28 2018-04-24 Amplipharm Pharmaceuticals, LLC Temozolomide powder formulation
WO2017189995A1 (en) 2016-04-28 2017-11-02 Amplipharm Pharmaceuticals, LLC Temozolomide powder formulation
US10285987B2 (en) 2017-04-28 2019-05-14 Amplipharm Pharmaceuticals, LLC Device and kit for dosing and dispensing non-liquid medicine
WO2017203365A1 (en) 2016-05-26 2017-11-30 Dr. Reddy's Laboratiories Ltd. Pharmaceutical compositions for treating acne
US11142775B2 (en) 2017-01-13 2021-10-12 University Of Iowa Research Foundation Bocaparvovirus small noncoding RNA and uses thereof
WO2018200034A1 (en) * 2017-04-28 2018-11-01 Amplipharm Pharmaceuticals, LLC Device and kit for dosing and dispensing non-liquid medicine
WO2019006287A1 (en) 2017-06-29 2019-01-03 Skyline Biosciences, Llc Isotretinoin oral-mucosal formulations and methods for using same
US10716774B1 (en) 2018-01-05 2020-07-21 Yale Pharmaceuticals LLC Pharmaceutical compositions containing isotretinoin with improved dissolution profile and enhanced stability
WO2022091140A1 (en) * 2020-11-01 2022-05-05 Idrs Labs Pvt Ltd Oral liquid pharmaceutical compositions of isotretinoin
US12016830B2 (en) 2022-07-01 2024-06-25 Acrotech Biopharma, LLC Pharmaceutical compositions comprising isotretinoin and processes for preparation and uses thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020025338A1 (en) * 2000-06-16 2002-02-28 Abha Pant Bioavailable dosage form of isotrentinoin

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA713539B (en) * 1970-06-23 1972-02-23 Hoffmann La Roche Pharmaceutical compositions
US4530213A (en) 1983-06-28 1985-07-23 Air Products And Chemicals, Inc. Economical and thermally efficient cryopump panel and panel array
US4678663A (en) * 1984-02-06 1987-07-07 Nuetrogena Corporation Hydroquinone composition having enhanced bio-availability and percutaneous adsorption
CA1282326C (en) 1984-12-14 1991-04-02 Paul J. Jarosz Pharmaceutical composition containing 13-cis vitamin a acid as the active ingredient
US5252604A (en) * 1992-07-10 1993-10-12 Hoffmann-La Roche Inc. Compositions of retinoic acids and tocopherol for prevention of dermatitis
US6054136A (en) 1993-09-30 2000-04-25 Gattefosse S.A. Orally administrable composition capable of providing enhanced bioavailability when ingested
US5993858A (en) * 1996-06-14 1999-11-30 Port Systems L.L.C. Method and formulation for increasing the bioavailability of poorly water-soluble drugs
US5993585A (en) * 1998-01-09 1999-11-30 Nike, Inc. Resilient bladder for use in footwear and method of making the bladder
US6020003A (en) * 1998-02-23 2000-02-01 Basf Corporation Method of making spray-dried powders with high edible-oil loadings based on non-hydrolyzed gelatin
FR2775597B1 (en) 1998-03-04 2001-04-20 Gattefosse Ets Sa ORAL PELLET ADAPTED TO IMPROVE THE BIOAVAILABILITY OF THE ACTIVE SUBSTANCE, METHOD OF MANUFACTURE
KR100336090B1 (en) * 1998-06-27 2002-05-27 윤승원 Solid dispersed preparation of poorly water-soluble drug containing oil, fatty acid or mixture thereof
PE20001227A1 (en) 1998-10-30 2000-11-06 Hoffmann La Roche PROCESSES TO PRODUCE AN ISOTRETINOIN COMPOSITION
WO2000025572A1 (en) 1998-11-04 2000-05-11 Jagjit Singh Kaurah Improved automatic plant watering system and water level control
US7374779B2 (en) * 1999-02-26 2008-05-20 Lipocine, Inc. Pharmaceutical formulations and systems for improved absorption and multistage release of active agents
US6294192B1 (en) 1999-02-26 2001-09-25 Lipocine, Inc. Triglyceride-free compositions and methods for improved delivery of hydrophobic therapeutic agents
US6267985B1 (en) * 1999-06-30 2001-07-31 Lipocine Inc. Clear oil-containing pharmaceutical compositions
US6248363B1 (en) * 1999-11-23 2001-06-19 Lipocine, Inc. Solid carriers for improved delivery of active ingredients in pharmaceutical compositions
US6383471B1 (en) 1999-04-06 2002-05-07 Lipocine, Inc. Compositions and methods for improved delivery of ionizable hydrophobic therapeutic agents
US6624154B1 (en) * 1999-04-23 2003-09-23 Bristol-Myers Squibb Company Compositions and methods for treatment of hyperproliferative diseases
US6593292B1 (en) * 1999-08-24 2003-07-15 Cellgate, Inc. Compositions and methods for enhancing drug delivery across and into epithelial tissues
US6267798B1 (en) * 2000-02-02 2001-07-31 Nuflux, Llc Composition for treating steel making slags
CA2423170A1 (en) 2000-09-22 2002-03-28 Galephar M/F Pharmaceutical semi-solid composition of isotretinoin
EP2432553A2 (en) 2009-05-20 2012-03-28 Ranbaxy Laboratories Limited Liquid dosage forms of isotretinoin
RU2400226C1 (en) 2009-06-08 2010-09-27 Юрий Степанович Макляков Method of treating acne

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020025338A1 (en) * 2000-06-16 2002-02-28 Abha Pant Bioavailable dosage form of isotrentinoin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9078925B2 (en) 2012-06-18 2015-07-14 Galephar Pharmaceutical Research, Inc. Pharmaceutical semi-solid composition of isotretinoin
WO2015094574A1 (en) * 2013-12-18 2015-06-25 Galephar Pharmaceutical Research, Inc. Pharmaceutical semi-solid composition of isotretinoin

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WO2002024172A1 (en) 2002-03-28
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US20080171084A1 (en) 2008-07-17

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